(Q33754592)

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Failure of fluid absorption in the endolymphatic sac initiates cochlear enlargement that leads to deafness in mice lacking pendrin expression

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scholarly article

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Europe PubMed Central

PubMed publication ID

29 July 2017

Failure of fluid absorption in the endolymphatic sac initiates cochlear enlargement that leads to deafness in mice lacking pendrin expression (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1 reference

based on heuristic

inferred from title

Philine Wangemann

2

object named as

Philine Wangemann

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Europe PubMed Central

PubMed publication ID

29 July 2017

author name string

Hyoung-Mi Kim

1

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Europe PubMed Central

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29 July 2017

language of work or name

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publication date

17 November 2010

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Europe PubMed Central

PubMed publication ID

29 July 2017

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Europe PubMed Central

PubMed publication ID

29 July 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

e14041

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

copyright license

Creative Commons Attribution 4.0 International

17 November 2010

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April 2022 Public Data File from Crossref

copyright status

0 references

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

1 reference

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21 June 2018

Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression

1 reference

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21 June 2018

Interferon-gamma suppresses Na+ -H+ exchanger in cultured human endolymphatic sac epithelial cells.

1 reference

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21 June 2018

Tonotopic gradient in the developmental acquisition of sensory transduction in outer hair cells of the mouse cochlea

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21 June 2018

Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?

1 reference

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21 June 2018

A protective role for type 3 deiodinase, a thyroid hormone-inactivating enzyme, in cochlear development and auditory function

1 reference

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21 June 2018

Free radical stress-mediated loss of Kcnj10 protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model

1 reference

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21 June 2018

Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2984494

21 June 2018

Lack of pendrin HCO3- transport elevates vestibular endolymphatic [Ca2+] by inhibition of acid-sensitive TRPV5 and TRPV6 channels

1 reference

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21 June 2018

Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential

1 reference

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21 June 2018

Co-expression of pendrin, vacuolar H+-ATPase alpha4-subunit and carbonic anhydrase II in epithelial cells of the murine endolymphatic sac

1 reference

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21 June 2018

Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2984494

21 June 2018

Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2984494

21 June 2018

Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study

1 reference

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21 June 2018

ASSOCIATION OF CONGENITAL DEAFNESS WITH GOITRE (PENDRED'S SYNDROME) A STUDY OF 207 FAMILIES.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2984494

21 June 2018

Developmental acquisition of sensory transduction in hair cells of the mouse inner ear

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2984494

21 June 2018

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness

1 reference

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21 June 2018

Hypothyroidism prevents developmental neuronal loss during auditory organ development

1 reference

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21 June 2018

Developmental and cellular expression pattern of epithelial sodium channel alpha, beta and gamma subunits in the inner ear of the rat.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2984494

21 June 2018

Development of monovalent ions in the endolymph in mouse cochlea.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2984494

21 June 2018

Type 2 iodothyronine deiodinase expression in the cochlea before the onset of hearing

1 reference

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21 June 2018

Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear

1 reference

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21 June 2018

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

1 reference

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21 June 2018

Effect of locally applied drugs on the endolymphatic sac potential

1 reference

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21 June 2018

Pendred syndrome--100 years of underascertainment?

1 reference

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21 June 2018

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

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Experimental blockage of the endolymphatic duct and sac and its effect on the inner ear of the guinea pig. A study on endolymphatic hydrops

1 reference

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An Experimental Approach to the Understanding and Treatment of Hereditary Syndromes with Congenital Deafness and Hypothyroidism

1 reference

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Quantification of the "in vitro" development of the mouse embryo inner ear

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Cation transport in the ampulla of the semicircular canal and in the endolymphatic sac.

1 reference

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Energization of sodium absorption by the H(+)-ATPase pump in mitochondria-rich cells of frog skin

1 reference

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The Slc26a4 transporter functions as an electroneutral Cl-/I-/HCO3- exchanger: role of Slc26a4 and Slc26a6 in I- and HCO3- secretion and in regulation of CFTR in the parotid duct.

1 reference

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30 October 2018

Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations.

1 reference

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Long-term follow-up of hearing loss in children and young adults with enlarged vestibular aqueducts: relationship to radiologic findings and Pendred syndrome diagnosis.

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SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.

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30 October 2018

ULTRASTRUCTURAL ORGANIZATION OF THE EPITHELIAL LINING IN THE ENDOLYMPHATIC DUCT AND SAC IN THE GUINEA PIG.

1 reference

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Neuro-otological findings in Pendred syndrome.

1 reference

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Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

1 reference

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1 reference

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Low-amiloride-affinity Na+ channel in the epithelial cells isolated from the endolymphatic sac of guinea-pigs

1 reference

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Intracellular and extracellular ion content of the endolymphatic sac.

1 reference

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Na,K-ATPase subunit isoform expression in the guinea pig endolymphatic sac

1 reference

https://pubmed.ncbi.nlm.nih.gov/21103348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for the presence of a Na+-H+ exchanger in the endolymphatic sac epithelium of guinea-pigs

1 reference

https://pubmed.ncbi.nlm.nih.gov/21103348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0014041

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

2010PLoSO...514041K

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

ResearchGate publication ID

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